Disease #03796 (ECTD11B (dysplasia, ectodermal, type 11B, hypohidrotic/hair/tooth, autosomal recessive (ECTD11B)), OMIM:614941)

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Official abbreviation	ECTD11B
Name	dysplasia, ectodermal, type 11B, hypohidrotic/hair/tooth, autosomal recessive (ECTD11B)
OMIM ID	614941
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	EDARADD
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-04-20 12:08:13 +02:00 (CEST)

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